NP-MRD: Showing NP-Card for 15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester (NP0339389)

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Record Information

Version

2.0

Created at

2024-09-11 21:35:21 UTC

Updated at

2024-09-11 21:35:21 UTC

NP-MRD ID

NP0339389

Secondary Accession Numbers

None

Natural Product Identification

Common Name

15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester

Description

15-Deoxy-delta12,14-Prostaglandin J2-2-glycerol ester, also known as 15-deoxy-δ12,14-PGJ2-2-glycerol ester, belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid. 15-Deoxy-delta12,14-Prostaglandin J2-2-glycerol ester is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02271200292D          

 28 28  0  0  1  0            999 V2000
    6.5190   -6.2307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1869   -5.7464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7733   -7.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8539   -6.2319    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5984   -7.0163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6388   -5.9776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2878   -7.6826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0828   -7.6841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9033   -7.5986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3877   -8.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0515   -9.0198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5359   -9.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1997  -10.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6841  -11.1089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3479  -11.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2514   -6.5301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0363   -6.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2085   -5.4690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9933   -5.2147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1655   -4.4079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9503   -4.1536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1225   -3.3468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5630   -4.7062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9073   -3.0925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0795   -2.2857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5200   -3.6450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8644   -2.0314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3048   -3.3908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  5  4  1  0  0  0  0
  4  6  1  6  0  0  0
  7  3  2  0  0  0  0
  8  5  2  0  0  0  0
  9  8  1  0  0  0  0
 10  9  2  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16  6  1  0  0  0  0
 17 16  2  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 21  2  0  0  0  0
 24 22  1  0  0  0  0
 25 24  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  1  0  0  0  0
 28 26  1  0  0  0  0
M  END


  Mrv0541 02271200292D          

 28 28  0  0  1  0            999 V2000
    6.5190   -6.2307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1869   -5.7464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7733   -7.0156    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8539   -6.2319    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5984   -7.0163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6388   -5.9776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2878   -7.6826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0828   -7.6841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9033   -7.5986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3877   -8.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0515   -9.0198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5359   -9.6877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1997  -10.4411    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6841  -11.1089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3479  -11.8623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2514   -6.5301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0363   -6.2759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2085   -5.4690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9933   -5.2147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1655   -4.4079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9503   -4.1536    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1225   -3.3468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.5630   -4.7062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9073   -3.0925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0795   -2.2857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5200   -3.6450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8644   -2.0314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.3048   -3.3908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  1  0  0  0  0
  5  4  1  0  0  0  0
  4  6  1  6  0  0  0
  7  3  2  0  0  0  0
  8  5  2  0  0  0  0
  9  8  1  0  0  0  0
 10  9  2  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16  6  1  0  0  0  0
 17 16  2  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 21  2  0  0  0  0
 24 22  1  0  0  0  0
 25 24  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  1  0  0  0  0
 28 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0339389

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC\C=C/C=C1/C(=O)C=C[C@@H]1C\C=C/CCCC(=O)OC(CO)CO

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O5/c1-2-3-4-5-6-10-13-21-19(15-16-22(21)26)12-9-7-8-11-14-23(27)28-20(17-24)18-25/h6-7,9-10,13,15-16,19-20,24-25H,2-5,8,11-12,14,17-18H2,1H3/b9-7-,10-6-,21-13+/t19-/m0/s1

> <INCHI_KEY>
JGKIBUMNHSZUSL-WZOKZYBXSA-N

> <FORMULA>
C23H34O5

> <MOLECULAR_WEIGHT>
390.5131

> <EXACT_MASS>
390.240624198

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
45.35153038781651

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,3-dihydroxypropan-2-yl (5Z)-7-[(1S,5E)-5-[(2Z)-oct-2-en-1-ylidene]-4-oxocyclopent-2-en-1-yl]hept-5-enoate

> <ALOGPS_LOGP>
4.44

> <JCHEM_LOGP>
4.2826068333333325

> <ALOGPS_LOGS>
-4.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.97907698548293

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.278238026294993

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9827691988008223

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
115.4742

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.36e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,3-dihydroxypropan-2-yl (5Z)-7-[(1S,5E)-5-[(2Z)-oct-2-en-1-ylidene]-4-oxocyclopent-2-en-1-yl]hept-5-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-FEB-12         0                                  
HETATM    1  C   UNK     0      12.169 -11.631   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.416 -10.727   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.643 -13.096   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.661 -11.633   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.184 -13.097   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.126 -11.158   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.737 -14.341   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      15.088 -14.344   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.619 -14.184   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.524 -15.431   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.896 -16.837   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.800 -18.084   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.173 -19.490   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      18.077 -20.737   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.449 -22.143   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      17.269 -12.190   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      18.734 -11.715   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      19.056 -10.209   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      20.521  -9.734   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      20.842  -8.228   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      22.307  -7.753   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      22.629  -6.247   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      23.451  -8.785   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      24.094  -5.773   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      24.415  -4.267   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      25.237  -6.804   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      25.880  -3.792   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0      26.702  -6.329   0.000  0.00  0.00           O+0
CONECT    1    2    3                                                       
CONECT    2    1    4                                                       
CONECT    3    1    5    7                                                  
CONECT    4    2    5    6                                                  
CONECT    5    3    4    8                                                  
CONECT    6    4   16                                                       
CONECT    7    3                                                            
CONECT    8    5    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16    6   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21   24                                                       
CONECT   23   21                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24   27                                                       
CONECT   26   24   28                                                       
CONECT   27   25                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   56    0
END

View in JSmol

Synonyms

Value	Source
15-Deoxy-δ12,14-prostaglandin J2-2-glycerol ester	Generator
15-Deoxy-Delta12,14-PGJ2-2-glycerol ester	HMDB
15-Deoxy-δ12,14-PGJ2-2-glycerol ester	HMDB
1,3-Dihydroxypropan-2-yl (5Z)-7-[(1S,5E)-5-[(2Z)-oct-2-en-1-ylidene]-4-oxocyclopent-2-en-1-yl]hept-5-enoic acid	Generator
15-Deoxy-δ-12,14-prostaglandin J2 2-glycerol ester	Generator

Chemical Formula

C₂₃H₃₄O₅

Average Mass

390.5131 Da

Monoisotopic Mass

390.24062 Da

IUPAC Name

1,3-dihydroxypropan-2-yl (5Z)-7-[(1S,5E)-5-[(2Z)-oct-2-en-1-ylidene]-4-oxocyclopent-2-en-1-yl]hept-5-enoate

Traditional Name

1,3-dihydroxypropan-2-yl (5Z)-7-[(1S,5E)-5-[(2Z)-oct-2-en-1-ylidene]-4-oxocyclopent-2-en-1-yl]hept-5-enoate

CAS Registry Number

Not Available

SMILES

CCCCC\C=C/C=C1/C(=O)C=C[C@@H]1C\C=C/CCCC(=O)OC(CO)CO

InChI Identifier

InChI=1S/C23H34O5/c1-2-3-4-5-6-10-13-21-19(15-16-22(21)26)12-9-7-8-11-14-23(27)28-20(17-24)18-25/h6-7,9-10,13,15-16,19-20,24-25H,2-5,8,11-12,14,17-18H2,1H3/b9-7-,10-6-,21-13+/t19-/m0/s1

InChI Key

JGKIBUMNHSZUSL-WZOKZYBXSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Prostaglandins and related compounds

Alternative Parents

Substituents

Prostaglandin skeleton
2-acyl-sn-glycerol
Monoradylglycerol
Monoacylglycerol
Fatty acid ester
Glycerolipid
Carboxylic acid ester
Cyclic ketone
Ketone
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Primary alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.44	ALOGPS
logP	4.28	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	14.28	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	115.47 m³·mol⁻¹	ChemAxon
Polarizability	45.35 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0013656

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB029626

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53481918

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester (NP0339389)

MOL for NP0339389 (15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester)

3D MOL for NP0339389 (15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester)

3D SDF for NP0339389 (15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester)

3D-SDF for NP0339389 (15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester)

PDB for NP0339389 (15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester)

3D PDB for NP0339389 (15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester)

SMILES for NP0339389 (15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester)

INCHI for NP0339389 (15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester)

Structure for NP0339389 (15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester)

3D Structure for NP0339389 (15-Deoxy-delta-12,14-prostaglandin J2 2-glycerol ester)